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Studies from a variety of scientific fields point at the importance of biofilms in the gut. For example, Jeffrey Gordon and colleagues,1 evaluating data from immunologists, environmental engineers and glycobiologists, proposed that “symbionts inhabiting the polysaccharide-rich mucus gel layer overlying the gut epithelium constitute a biofilm-like community and that retention in such a matrix benefits the host by promoting functions served by the microbiota, including digestion of luminal contents and fortification of host defenses.” Evaluating our own immunological data, data from microbiologists and the medical literature, we independently came to the same conclusions.2
Direct observations of biofilms in the normal gut were lacking as recently as five years ago, probably because preservation of the epithelial glycocalyx, like the preservation of other glycocalyx structures, is technically challenging, as has long been known.3–5 In fact, we have found that manipulations as seemingly innocuous as washing with saline can disrupt biofilms from normal bowel tissue.6 With this in mind, we devised an approach that reproducibly preserves biofilms in the normal, unprepped (without flushing of the luminal contents) bowel,6 and examined fresh, unprepped human appendixes that had been removed from recipients during kidney–pancreas transplant procedures. Our laboratory has subsequently recapitulated our previously published observations using a fresh, normal, unprepped human appendix from a deceased organ donor (fig 1). To date, biofilms have been observed in the normal proximal (not distal) large bowel of mice,7 rats,6 baboons6 and humans.6 Thus, although enteric biofilms are likely in a steady state of shedding and regrowth, and although the percentage of epithelium covered with biofilms is unknown, there is no doubt that biofilms are indeed present in the normal bowel.
In a recent article (Gut 2007;56:343–50) Alexander Swidsinski and colleagues flatly dispute our findings of biofilms in the human appendix, referring to our work as “fiction”. The investigators, following a 6-hour fixation procedure with a non-aqueous solvent, find no biofilms in the human appendix and conclude that biofilms do not exist in the normal human bowel. We do not dispute or doubt the observations made by Swidsinski et al., since their results confirm what we have already demonstrated: biofilms in the normal colon are not stable using common preservation techniques.6
Of interest is the fact that Swidsinki’s laboratory has been successful at preserving biofilms in biopsies of the diseased bowel of humans,8,9 in the normal bowel of laboratory mice,7 but not in the normal human appendix (Gut 2007;56:343–50). A likely explanation for these observations is that, for technical reasons, some tissues were more effectively preserved than others. The idea that the typically thick-walled appendix is particularly difficult to preserve is supported by the fact that Swidsinski and colleagues used a 6-hour fixation procedure for the appendix, but only a 2-hour procedure for the biopsy samples. Another potential explanation for the observations made by Swidsinski’s laboratory is that biofilms in the diseased human bowel may be more resilient than biofilms in the normal human gut. Indeed, biofilm formation in the normal bowel is probably supported by the immune system,10–12 and since inflammatory bowel disease is associated with an enhanced immune response, it is not surprising that biofilm formation in the diseased state would be profoundly increased.
Finally, we would point out that it is not overly surprising to observe biofilms in the normal colons of humans since similar observations have been made in the normal colons of laboratory animals as diverse as mice7 (observations from Swidsinski’s own laboratory) and baboons6 (observations from our laboratory).
Competing interests: None.
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